Search results for "Reactivity"

showing 10 items of 880 documents

1,3-Dipolar cycloaddition of 1H-pyrazinium-3-olate and N1- and C-methyl substituted pyrazinium-3-olates with methyl acrylate: a density functional th…

2011

Abstract A DFT study of the 1,3-dipolar cycloaddition of methyl acrylate to 1H-pyrazinium-3-olate and N1- and C-methyl substituted pyrazinium-3-olates, in the gas phase and in THF, has been carried out at the B3LYP/6-31G(d) level. Two stereoisomeric pathways, endo and exo, and two regioisomeric channels, 2-oxo-3,8-diazabicyclo[3.2.1]octane-6-ester and 7-ester products, have been considered. Thermodynamic and kinetic parameters calculated at room temperature have been analyzed. The regioselectivity has been interpreted using reactivity indices. It is generally found that the exo pathway is preferred and the formation of the 6-esters is dominant. The theoretical data obtained for the cycloadd…

Organic ChemistryRegioselectivityBiochemistryMedicinal chemistryCycloadditionGas phasechemistry.chemical_compoundchemistryDrug Discovery13-Dipolar cycloadditionStructural isomerOrganic chemistryReactivity (chemistry)Density functional theoryMethyl acrylateTetrahedron
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High-pressure NMR spectroscopy: An in situ tool to study tin-catalyzed synthesis of organic carbonates from carbon dioxide and alcohols. Part 2 [1]

2015

Dialkoxide diorganotin(IV) complexes are known to readily react with carbon dioxide under pressure and they are considered as suitable catalyst precursor models for the direct synthesis of organic carbonates. To gain a better understanding of CO2 insertion processes with Sn-OR bonds, the reactivity of n-Bu2Sn(OCH(CH3)(2))(2) (2) was investigated using high-pressure NMR (HP-NMR) spectroscopy. In deuterated solvents (isopropanol-d(8) and toluene-d(8)) under 50 bar of CO2 pressure at 80 degrees C, Sn-119{H-1} NMR experiments revealed the exclusive formation of an unprecedented tetraorganodistannoxane species, characterized as the bis[diisopropycarbonatotetrabutyldistannoxane] complex, {[n-Bu2S…

Organic carbonatesOrganic ChemistryInorganic chemistrychemistry.chemical_elementNuclear magnetic resonance spectroscopyBiochemistryCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryDeuteriumTetraorganodistannoxaneCarbon dioxidePolymer chemistrySn-119 NMR spectraMaterials ChemistryHigh pressure NMR spectroscopyReactivity (chemistry)Physical and Theoretical ChemistryTinSpectroscopyCarbon dioxide utilizationDiorganotin(IV)Bar (unit)Journal of Organometallic Chemistry
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Carbon–Phosphorus Coupling from C^N Cyclometalated Au III Complexes

2020

Abstract With the aim of exploiting new organometallic species for cross‐coupling reactions, we report here on the AuIII‐mediated Caryl−P bond formation occurring upon reaction of C^N cyclometalated AuIII complexes with phosphines. The [Au(C^N)Cl2] complex 1 featuring the bidentate 2‐benzoylpyridine (CCON) scaffold was found to react with PTA (1,3,5‐triaza‐7‐phosphaadamantane) under mild conditions, including in water, to afford the corresponding phosphonium 5 through C−P reductive elimination. A mechanism is proposed for the title reaction based on in situ 31P{1H} NMR and HR‐ESI‐MS analyses combined with DFT calculations. The C−P coupling has been generalized to other C^N cyclometalated Au…

Organometallic Chemistrygold(III) cyclometalataled compoundsDenticitygold(III) cyclometalated compoundschemistry.chemical_element010402 general chemistry01 natural sciencesMedicinal chemistryDFTCatalysisReductive eliminationchemistry.chemical_compoundcross-couplingcarbon-phosphorous bond[CHIM]Chemical SciencesReactivity (chemistry)Phosphonium010405 organic chemistryPhosphorusCommunicationOrganic Chemistryreductive eliminationGeneral ChemistryBond formationcross- couplingCommunications0104 chemical sciences3. Good healthddc:gold(III) cyclometalataled compoundchemistrySettore CHIM/03 - Chimica Generale E Inorganicadensity functional calculationscarbon–phosphorous bondCarbon
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Room temperature ionic liquids structure and its effect on the mononuclear rearrangement of heterocycles: an approach using thermodynamic parameters.

2006

The kinetics of the rearrangement of the Z-phenylhydrazone of 3-benzoyl-5-phenyl-1,2,4-oxadiazole (1) into the relevant 4-benzoylamino-2,5-diphenyl-1,2,3-triazole (2) induced by amines have been studied in five room-temperature ionic liquids (RTILs) at different temperatures. The kinetic data collected show that both cationic and anionic parts of RTILs significantly influence the reactivity of the title reaction. The calculated activation parameters allow us to advance hypotheses about the weak interactions operating in RTIL solutions.

OxadiazolesMolecular StructureOrganic ChemistryKineticsCationic polymerizationHydrazonesTemperatureIonic Liquidsionic liquids base catalysis MHR reactionTriazolesKinetic energyIonchemistry.chemical_compoundchemistryHeterocyclic CompoundsIonic liquidOrganic chemistryPhysical chemistryMoleculeThermodynamicsReactivity (chemistry)Amine gas treatingAminesThe Journal of organic chemistry
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On the Rearrangement in Dioxane/Water of (Z)-Arylhydrazones of 5-Amino-3-benzoyl-1,2,4-oxadiazole into (2-Aryl-5-phenyl-2H-1,2,3-triazol-4-yl)ureas: …

2006

We have recently evidenced an interesting differential behavior in the reactivity in dioxane/water between the (Z)-2,4-dinitrophenylhydrazone (1a) and the (Z)-phenylhydrazone (1b) of 5-amino-3-benzoyl-1,2,4- oxadiazole. The former rearranges into the relevant triazole 2a only at pS+ > 4.5 while undergoing hydrolysis at high proton concentration (pS+ < 3.5); on the contrary, the latter rearranges into 2b in the whole pS+ range examined (0.1 e pS+ e 14.9). Thus, for a deeper understanding of these differences we have now collected kinetic data on the rearrangement in dioxane/water of a series of 3- or 4-substituted (Z)-phenylhydrazones (1c-l) of 5-amino-3-benzoyl-1,2,4-oxadiazole in a wide ra…

OxadiazolesMolecular StructureStereochemistryArylOrganic ChemistryHydrazonesTriazoleSubstituentWaterOxadiazolemononuclear rearrangement of heterocycles acid catalysis base catalysisTriazolesChemical synthesisMedicinal chemistryCatalysisDioxanesKineticschemistry.chemical_compoundAcid catalysischemistryThermodynamicsAmine gas treatingReactivity (chemistry)
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Synthesis and reactivity of cristobalite obtained from the SiO2-V2O5 system

1990

On etudie par diffraction RX l'evolution des phases cristallines lors de la cuisson a 650-1250 o C de compositions du systeme ZrO 2 −V 2 O 5 −SiO 2 et la reactivite de la cristobalite preparee avec la phase ZrO 2 monoclinique

Oxide ceramicsMaterials scienceInorganic chemistryX-ray crystallographyPhysical chemistryGeneral Materials ScienceReactivity (chemistry)CristobaliteJournal of Materials Science Letters
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Photochemistry and Non-adiabatic Photodynamics of the HOSO Radical

2021

6 pags., 2 figs.

Ozonebusiness.industryChemistryGeneral ChemistryPhotochemistryBiochemistryQuantum chemistryCatalysisAtmospherechemistry.chemical_compoundColloid and Surface ChemistryReactivity (chemistry)GeoengineeringbusinessAdiabatic processStratosphereJournal of the American Chemical Society
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Involvement of distal airways in a chronic model of experimental asthma.

2005

Summary Background Bronchial asthma is characterized by chronic airway inflammation and airway remodelling which occurs in both proximal and distal airways. These changes are associated with development of airway hyper-responsiveness and airflow limitation. Objective This study was aimed to analyse whether chronic inhalative allergen challenges in mice lead to morphological and physiological changes comparable with this phenotype. Methods For this purpose, BALB/c mice were systemically sensitized to ovalbumin (OVA) followed by aerosol allergen challenges on 2 consecutive days per week for 12 weeks. Results In chronically challenged mice, tissue inflammation in proximal as well as distal air…

Pathologymedicine.medical_specialtyAllergyOvalbuminImmunologyInflammationBronchiMiceTransforming Growth Factor betaAdministration InhalationmedicineImmunology and AllergyAnimalsRespiratory systemAsthmaMice Inbred BALB CMucous MembraneInhalationbusiness.industryRespiratory diseaserespiratory systemAllergensmedicine.diseaseAsthmarespiratory tract diseasesDisease Models Animalmedicine.anatomical_structureImmunologyChronic DiseaseDisease ProgressionCytokinesFemalemedicine.symptomBronchial HyperreactivityAirwaybusinessBronchoalveolar Lavage FluidRespiratory tractClinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology
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Structural characterization of Pd-Ag and Pd-Cu bimetallic catalysts by means of EXAFS, WAXS and XPS

2000

Bimetallic Pd-Ag and Pd-Cu pumice-supported catalysts have been synthesized following different preparation procedures with the aim of improving the selectivity and reactivity of monometallic Pd/pumice systems. The structural characterization, carried out by X-ray Diffraction, X-ray Absorption and X-ray Photoelectron Spectroscopy, allowed to investigate the importance of the preparation procedures in the alloy formation.

Pd-CuMaterials scienceExtended X-ray absorption fine structureAlloyengineering.materialCatalysisCrystallographyX-ray photoelectron spectroscopyPd-AgengineeringPhysical chemistrybimetallic catalystsReactivity (chemistry)Absorption (chemistry)SelectivityBimetallic strip
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Importance of iron and aluminium in rapid and slow combustion of peat

1990

Abstract The effects of Fe and Al on peat combustion and the formation of nitrogen oxides were studied under conditions of rapid combustion in an entrained flow reactor, and under conditions of slow combustion in a thermobalance and a differential scanning calorimeter. Iron had a strong catalytic effect on both the slow and rapid combustion, and it decreased the ratio of N2O to NO in the combustion gases. A decrease in the content of inorganic compounds decreased reactivity, probably because of the decrease in iron content. Aluminium did not have a detectable catalytic effect on the combustion rate but it depressed the formation of nitrogen oxides slightly. The chemical treatment to increas…

PeatChemical treatmentGeneral Chemical EngineeringOrganic ChemistryEnergy Engineering and Power Technologychemistry.chemical_elementCombustionFuel TechnologyDifferential scanning calorimetrychemistryChemical engineeringAluminiumIron contentComposition (visual arts)Reactivity (chemistry)Nuclear chemistryFuel
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